Results 31 to 40 of about 312 (131)
Multiple apocrine hidrocystomas
A 83-year-old woman presented with a 7-year history of translucent papules that were scattered diffusely over her nose, peri-orbital region, and cheeks. These lesions were exacerbated by heat and exercise. Histopathologic examination of a biopsy specimen from the cheek showed a thin-walled cyst lined by a flattened bi-layered epithelium that exhibited ...
Anandasabapathy, Niroshana +1 more
openaire +4 more sources
Primary cutaneous mucinous carcinoma (PCMC) is a rare, low‐grade malignant neoplasm of the sweat gland, whose history has been controversial regarding eccrine versus apocrine origin. This case report describes a 53‐year‐old male who presented to the University of Florida, Gainesville, ophthalmology clinic and was referred to the oculoplastics service ...
Stephanie M. Tillit +4 more
wiley +1 more source
Orbital apocrine hidrocystoma with immunohistochemical confirmation
The authors report the first case in Brazilian literature of orbital apocrine hidrocystoma with immunohistochemistry confirmation. The tumor had been growing slowly and progressively, there was no history of impaired vision, diplopia, watering, discharge,
Eduardo Damous Feijó +6 more
doaj +1 more source
A New Case of Hybrid Epidermoid and Apocrine Cyst
We described a new case of a hybrid epidermoid and apocrine cyst, known to be a rare histopathological entity. The cyst was located in the axillary region and completely excised, without complication.
Fulvia Serra, Gürkan Kaya
doaj +1 more source
Congenital sudoriferous cyst of the orbit: A case report and review of literature
Apocrine gland cyst (sudoriferous cyst and apocrine hidrocystoma) is fairly uncommon in the eyelid, where it derives from the apocrine glands of Moll. In rare instances, an apocrine gland cyst can occur in the anterior portion of the orbit. If an orbital
Parit S Ladani +3 more
doaj +1 more source
Schopf–Schulz–Passarge syndrome
Schopf–Schulz–Passarge syndrome (SSPS) is a rare type of ectodermal dysplasia that has autosomal recessive inheritance. It is characterized by palmoplantar keratoderma, hypodontia, hypotrichosis, nail dystrophy, and multiple periocular and eyelid ...
Kinjal D Rambhia +3 more
doaj +1 more source
Apocrine hidrocystomas (AHC) are uncommon cystic lesions of apocrine glands and are most often solitary. They are usually found in the head and neck region. Multiple AHC have been rarely reported in the literature usually in the eyelids and face.
Shailaja Shukla +3 more
doaj +1 more source
Apocrine Hidrocystoma of the Parotid Gland
Apocrine hidrocystoma is a cystic tumor originating from apocrine sweat glands. It is predominantly located in the eyelid margins. Here, we report a case of apocrine hidrocystoma of the parotid gland in a 19-year-old man who was referred to our outpatient clinic with a 5-year history of a gradual swelling in the left parotid region.
Ines Kharrat +7 more
openaire +2 more sources
Clinicopathological study of cutaneous adnexal cyst with some unusual presentation
Background: Cutaneous cysts are slow-growing benign intradermal or subcutaneous tumors that occur commonly in the hair-bearing areas of the body. Sometimes they occur in non-hair-bearing areas due to traumatic implantation of the epidermis.
Praneeta Jaswant Singh, Himani Dahiya
doaj +1 more source
Endocrine Mucin‐Producing Sweat Gland Carcinoma, a Histological Challenge
Endocrine mucin‐producing sweat gland carcinoma (EMPSGC) is a rare adnexal tumor of the skin with low‐grade cytological features and neuroendocrine differentiation. It has a predilection for the skin of the eyelid, but has also been reported in the face and rarely extra‐facial locations. The tumor is seen more frequently in women and on average affects
Mary Anne Brett +4 more
wiley +1 more source

